Used primarily in the synthesis of antifungal medications, particularly as an intermediate in the production of structurally complex agents targeting Candida and Aspergillus species. Its chiral structure enhances binding selectivity to fungal cell membrane components, improving efficacy and reducing off-target effects. Also employed in research settings to develop novel derivatives with improved pharmacokinetic profiles, including better metabolic stability and tissue penetration. The presence of trifluoromethyl and hydroxydiphenyl groups contributes to lipophilicity, aiding in membrane interaction and antifungal activity.